Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73569008-73569286 | Rare:62 | ||||
chr14:73787146-73787371 | Common:2; Rare:83 | ||||
chr14:73790084-73790233 | Rare:28 | ||||
chr14:73851741-73852001 | Common:5; Rare:88 | ||||
chr14:73886765-73886869 | Common:1; Rare:33 | ||||
chr14:73950062-73950333 | Common:6; Rare:117; Clinvar (benign):4 | ||||
chr14:74019256-74019436 | Common:1; Rare:72 | ||||
chr14:74493240-74493788 | Common:4; Rare:176; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr14:74713049-74713200 | Rare:87 | ||||
chr14:75002644-75002996 | Common:1; Rare:115; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr14:75126908-75127081 | Rare:65 | ||||
chr14:75176356-75176564 | Rare:50 | ||||
chr14:75176566-75176813 | Common:1; Rare:72 | ||||
chr14:75660813-75661299 | Common:4; Rare:113 | ||||
chr14:77376989-77377410 | Common:5; Rare:126 |